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MET642 for Non-alcoholic Fatty Liver Disease

Phase 2
Waitlist Available
Research Sponsored by Metacrine, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 28 days after last dose
Awards & highlights

Study Summary

This study is evaluating whether a drug called MET642 can improve liver function in people with nonalcoholic steatohepatitis (NASH).

Eligible Conditions
  • Non-alcoholic Fatty Liver Disease

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 28 days after last dose
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 28 days after last dose for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Adverse Events
ECG
Laboratory tests
+1 more
Secondary outcome measures
Pharmacodynamic Profile of MET642
Pharmacokinetic Profile of MET642
Pharmacological Activity of MET642

Trial Design

3Treatment groups
Experimental Treatment
Placebo Group
Group I: MET642 low doseExperimental Treatment1 Intervention
Group II: MET642 high doseExperimental Treatment1 Intervention
Group III: MET642 PlaceboPlacebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
MET642
2021
Completed Phase 2
~220

Find a Location

Who is running the clinical trial?

Metacrine, Inc.Lead Sponsor
1 Previous Clinical Trials
120 Total Patients Enrolled
1 Trials studying Non-alcoholic Fatty Liver Disease
120 Patients Enrolled for Non-alcoholic Fatty Liver Disease

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~53 spots leftby Apr 2025